{{Rsnum
|rsid=121912711
|Chromosome=5
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=ALDH7A1
|position=126561094
|Gene_s=ALDH7A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=107323
|rsnum=121912711
|variant=0008
}}{{ClinVar
|rsid=121912711
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=125896786
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ALDH7A1:501
|GENE_NAME=ALDH7A1
|GENE_ID=501
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.125896786T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=107323.0008
|CLNSIG=5
|CLNCUI=C1849508
|CLNDBN=Pyridoxine-dependent epilepsy
|Disease=Pyridoxine-dependent epilepsy
|CLNACC=RCV000019617.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1486:C1849508:266100:3006
}}